Adeline Serckx

Devastating Decline of Forest Elephants in Central Africa

African forest elephants– taxonomically and functionally unique–are being poached at accelerating rates, but we lack range-wide information on the repercussions. Analysis of the largest survey dataset ever assembled for forest elephants (80 foot-surveys; covering 13,000 km; 91,600 person-days of fieldwork) revealed that population size declined by ca. 62% between 2002–2011, and the taxon lost 30% of its geographical range. The population is now less than 10% of its potential size, occupying less than 25% of its potential range. High human population density, hunting intensity, absence of law enforcement, poor governance, and proximity to expanding infrastructure are the strongest predictors of decline. To save the remaining African forest elephants, illegal poaching for ivory and encroachment into core elephant habitat must be stopped. In addition, the international demand for ivory, which fuels illegal trade, must be dramatically reduced.

Bonobo nest site selection and the importance of predictor scales in primate ecology

The role of spatial scale in ecological pattern formation such as the geographical distribution of species has been a major theme in research for decades. Much progress has been made on identifying spatial scales of habitat influence on species distribution. Generally, the effect of a predictor variable on a response is evaluated over multiple, discrete spatial scales to identify an optimal scale of influence. However, the idea to identify one optimal scale of predictor influence is misleading. Species‐environment relationships across scales are usually sigmoid increasing or decreasing rather than humped‐shaped, because environmental conditions are generally highly autocorrelated. Here, we use nest count data on bonobos (Pan paniscus) to build distribution models which simultaneously evaluate the influence of several predictors at multiple spatial scales. More specifically, we used forest structure, availability of fruit trees and terrestrial herbaceous vegetation (THV) to reflect environmental constraints on bonobo ranging, feeding and nesting behaviour, respectively. A large number of models fitted the data equally well and revealed sigmoidal shapes for bonobo‐environment relationships across scales. The influence of forest structure increased with distance and became particularly important, when including a neighbourhood of at least 750 m around observation points; for fruit availability and THV, predictor influence decreased with increasing distance and was mainly influential below 600 and 300 m, respectively. There was almost no difference in model fit, when weighing predictor values within the extraction neighbourhood by distance compared to simply taking the arithmetic mean of predictor values. The spatial scale models provide information on bonobo nesting preferences and are useful for the understanding of bonobo ecology and conservation, such as in the context of mitigating the impact of logging. The proposed approach is flexible and easily applicable to a wide range of species, response and predictor variables and over diverse spatial scales and ecological settings.

Feeding ecology of bonobos living in forest-savannah mosaics: Diet seasonal variation and importance of fallback foods.

Primates along with many other animal taxa are forced to cope with large shifts in basic ecological conditions because of rapid anthropogenically induced changes of their habitats. One of the coping strategies for primates is to adjust their diet to these changes, and several studies have demonstrated the importance of fallback resources for this. Bonobos, like chimpanzees, might be particularly vulnerable to habitat fragmentation because of their high dependence on fruit availability. Little is known, however, about bonobo feeding ecology in fragmented habitats and their use of fallback resources. In this study, we investigate diet seasonal variation and the exploitation of preferred and fallback foods in a bonobo population living in forest‐savannah mosaics. Results show that bonobos have adapted to this fragmented habitat by feeding on only a few fruit species, including an important number of non‐tree species (liana, herb and savannah shrub), in comparison to populations living in dense forests. These non‐tree plants have been defined as fallback and non‐preferred foods, which are most probably consumed to maintain high frugivory. Interestingly, we identified that preferred foods are all typical of mature forests while fallback resources are mainly found in forest edges or disturbed areas. This finding indicates that bonobos prefer to use mature forests when feeding, as they do for nesting, but extend their range use to forest areas in close proximity to humans when the availability of preferred fruits is low. Finally, we show that bonobo diet relies heavily on two abundant fallback fruits: Musanga cecropioides and Marantochloa leucantha. Other studies have demonstrated that the selection of abundant fallback resources enables primates to subsist at high densities and to maintain cohesive groups, as observed at this study site. Our findings suggest that bonobos living in forest‐savannah mosaics can be considered as staple fallback food consumers. Am. J. Primatol. 77:948–962, 2015.

Optimizing scale search in species distribution models

DOI: 10.1159/000354129 298 5th Congress of the European Federation for Primatology researchers usually argue that one of the distinguishing features of non-human primates’ gestures is their high degree of flexibility, which can be considered in different ways: (1) ‘means-end dissociation’, which refers to the use of a particular gesture in different functional contexts and/or several gestures for one specific context, and (2) gesture sequences which consist of combinations of two or more gestural signals. Both strategies enable non-human primates to adjust their gesture use to their partner’s behaviour and to increase the range of potential meanings that can be conveyed by combining the components of a more or less limited gestural repertoire. Because of their flexible use, however, very few gestures have a specific meaning, but their meaning is defined by the context in which they occur. Thus, in contrast to many vocalizations of non-human primates, their gestures are (1) less context-specific and do not represent functionally referential signals and, related to this, (2) gesture sequences do not represent meaningful combinations used for other functions than their single components. Therefore, I will first provide an overview of recent research on the flexible use of gestures in great apes to demonstrate how they create meaning in their interactions with others. I will then discuss how these findings relate to evidence from vocal studies with the aim to identify ‘blind spots’ and biases that currently constrain a fruitful debate about the origins of human language.Comparative studies of primate grasping and manipulative behaviours in captivity are numerous but there has been little research on hand use in the wild. Hand use during wild non-locomotor behaviours may reveal increased ranges of joint mobility or manipulative behaviours that have been previously ignored or underestimated. Manipulative behaviours in apes can strongly correlate with different habitats at the species and population level. Chimpanzees more often use tools in the wild and thus are thought to be more manipulative than gorillas. However, captive studies have demonstrated high dexterity in both taxa. We investigate hand use during manipulation (e.g. food processing, tool-use) in wild mountain gorillas (Gorilla beringei, Bwindi Impenetrable National Park, Uganda) and wild chimpanzees (Pan troglodytes verus, Tai National Park, Cote d’Ivoire). We used video data collected in the wild that included 32 gorilla (n=9 individuals) and 53 chimpanzee (n=11 individuals) instances of manipulative tasks. Digital images were extracted and analysed frame by frame. Preliminary results show that hand grips are similar between gorillas and chimpanzees during the manipulation of common food objects, such as long plant stems or branches. During the manipulation of species-specific food objects, gorillas use variable thumb-index grips during the manipulation of thistles and small plant stems, while chimpanzees use similar grips during nut-cracking. These preliminary results suggest that Bwindi mountain gorillas have similarly high dexterity as that of Tai chimpanzees despite not being tool-users. Gorillas frequently use precision grasping more to obtain small rather than large food items, which is similar to chimpanzees and other non-human primates.Previous studies have shown a positive relationship between proximity to humans or habitat fragmentation and parasitic levels in non-human primates (NHPs). However, to date few have explicitly explored links between parasite load and stress conditions. To better understand the links between parasite prevalence and NHP immune system efficiency and stress levels, faecal samples of Alouatta palliata and the critically endangered Ateles geoffroyi geoffroyi were non-invasively collected in northern Costa Rica. We investigated whether the presence of gastrointestinal parasites was related to the abundance of hormones (cortisol and testosterone). Samples were gathered across three areas differing in the frequency and diversity of human presence, i.e. around the Cano Palma Biological Station, near villages and at ecotourism sites. Two grams of each faecal sample were stored in a sugar saturated solution with 10% formalin to conserve the parasites; the remaining matter was dried to preserve DNA and steroid hormones. The samples enabled the quantification of parasites as well as testosterone and cortisol levels using ELISA as proxies of general health status and stress levels. Data on parasite abundance and hormone levels were contrasted across the two species and the three different sampling areas. Furthermore, we assessed the genetic exchange among the different groups of primates sampled. We genetically analysed the samples using 12 microsatellites previously validated by the University of Costa Rica. We verified whether transmission of parasites among the groups could be possible concomitant to the genetic exchange. This study aimed to better understand and assess the impact of human factors on NHP health and across NHPs with different socio-ecological characteristics.DOI: 10.1159/000354129 290 5th Congress of the European Federation for Primatology considerably between species for any given body size. Numerous hypotheses have been put forward to explain this variation. In recent years, we have tested predictions that flow from a framework focusing on the energetic aspects of having a large amount of the metabolically expensive brain tissue. In this talk, I will give an overview of our findings from broad comparative phylogenetic studies in mammals, and their implications for our understanding of non-human and human primate evolution. In sum, we found evidence for two pathways to increase relative brain size compared to the ancestral state. First, a species may change its lifestyle to allow for a stable increase in its total energy budget, e.g. by changing its diet. Alternatively, or in combination with the first pathway, a species may allocate more energy to the brain and less to other expensive functions such as offspring production. Ultimately, this option results in very low population growth rates even in good conditions, as found in great apes. A further increase in brain size would not be compatible with demographically viable populations in these large-brained primates. However, using comparative evidence from mammals, we demonstrate that help from non-mothers can alleviate this trade-off between reproductive effort and brain size. Nevertheless, the energetic constraints on brain size evolution will only be overcome in species that can actually benefit from enhanced cognitive abilities. While such benefits are potentially ubiquitous, we would expect them to be undermined by unavoidable mortality in some socioecological conditions, and by the difficulty of transferring knowledge across generations in some social systems. A combined test of all these considerations remains a challenge, largely due to the shortcomings of the distinct datasets, but I will present the newest data and results from our current projects.Throughout their range across Africa, chimpanzees (Pan troglodytes) are threatened with extinction due to habitat destruction, disease and unsustainable levels of hunting and capture, in spite of being protected by national and international laws. In recent years, the bush meat and the pet trade have resulted in a significant increase in the number confiscated orphan chimpanzees. The Chimpanzee Conservation Centre (CCC), located in the High Niger National Park (HNNP), is the only Pan African Sanctuary Alliance (PASA)-accredited sanctuary caring for chimpanzee orphans in Guinea, West Africa. This sanctuary has been rehabilitating confiscated chimpanzees since 1997. With the aim of reinforcing the wild chimpanzee population of the HNNP and to enhance park protection, the CCC, in 2008, released a first group of 12 chimpanzees into the Mafou core area of the park. Five of those individuals have since settled at the release site and continue to be monitored. In August 2011, the CCC was able to re-enforce this resident group with the successful addition of 2 adult females. Post-release monitoring of these individuals involved distance monitoring using simple VHF and/or ARGOS and GPS store-on-board radio collars. Here, we present data downloaded in 2011–2012 from the GPS store-on-board collars of 2 adult males and these 2 additional adult females. These data allowed us to analyse their social dynamics, party composition, habitat preferences, day range and home range use. Our results indicate that these females integrated successfully into the resident group and that the behaviour of these wild-born released orphan chimpanzees mirrors that of wild counterparts inhabiting similar savannah dominated landscapes, suggesting that they have adapted appropriately to their release conditions.